FDA applicant
Life-Tech Instruments, Inc.
FDA records 19 decisions for Life-Tech Instruments, Inc. (Mchenry, IL) from 1977 to 1981: 19 510(k) clearances. Most are in product codes IKN (Electromyograph, Diagnostic) and GWJ (Stimulator, Auditory, Evoked Response). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Life-Tech Instruments, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Life-Tech Instruments, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
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